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• W3024656876 endingPage "396" @default.
• W3024656876 startingPage "369" @default.
• W3024656876 abstract "Alterations in the homeostasis of several adhesion GPCRs (aGPCRs) have been observed in cancer. The main cellular functions regulated by aGPCRs are cell adhesion, migration, polarity, and guidance, which are all highly relevant to tumor cell biology. Expression of aGPCRs can be induced, increased, decreased, or silenced in the tumor or in stromal cells of the tumor microenvironment, including fibroblasts and endothelial and/or immune cells. For example, ADGRE5 (CD97) and ADGRG1 (GPR56) show increased expression in many cancers, and initial functional studies suggest that both are relevant for tumor cell migration and invasion. aGPCRs can also impact the regulation of angiogenesis by releasing soluble fragments following the cleavage of their extracellular domain (ECD) at the conserved GPCR-proteolytic site (GPS) or other more distal cleavage sites as typical for the ADGRB (BAI) family. Interrogation of in silico cancer databases suggests alterations in other aGPCR members and provides the impetus for further exploration of their potential role in cancer. Integration of knowledge on the expression, regulation, and function of aGPCRs in tumorigenesis is currently spurring the first preclinical studies to examine the potential of aGPCR or the related pathways as therapeutic targets." @default.
• W3024656876 created "2020-05-21" @default.
• W3024656876 creator A5018778245 @default.
• W3024656876 creator A5050616688 @default.
• W3024656876 creator A5056151621 @default.
• W3024656876 creator A5090162618 @default.
• W3024656876 date "2016-01-01" @default.
• W3024656876 modified "2023-10-14" @default.
• W3024656876 title "Adhesion GPCRs in Tumorigenesis" @default.
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